URS-1K – Ketone Test Strips (100 Strips)
- Acetoacetic acid
- Fast read in 15 seconds
- Convenient flip top vial
- Suitable for low carb dieters
- Customer Reviews
Urine Ketone Test Strips are made for urinalysis of both qualitative and semi-quantitative, it test ketone in urine to detect the metabolites of fat.
Kketone Strips are looking for acetoacetic acid in the urine. This acid reacts with nitroprusside, a chemical in the strip, to produce a color. This color corresponds with a chart that comes packaged along with your test strips, usually on the outside of the vial. Typically, the results include negative, trace, moderate or large ketones.
100 Strips/bottle, 200 bottles/ctn
Urinalysis Reagent Strip Instruction of Use
Urinalysis Reagent Strips are made for urinalysis of both qualitative and semi-quantitative, which are in vitro reagent for diagnostics. It tests Leukocytes, Nitrite, Urobilinogen, Protein, pH, Blood, Specific Gravity, Ascorbic Acid, Ketone, Bilirubin, Glucose, Microalbumin in urine. Please refer to the out-side box and bottle label for the specific test parameters of the product you are using.
Please read this direction carefully before using.
The results on the strips can be read visually and instrumentally.
Specimen Collection and Preparation
Use only clean dry container to collect urine and should be shocked before testing and test it within 2 hours. Any operations must be in the sanitary environment.
Water cannot be used as negative quality control liquid. Antiseptic of urine cannot prevent the ketone, bilirubin and urobilinogen from deteriorated. For the long time urine specimen, the test results of glucose, pH, nitrite and blood can be affected cause of bacterial growth.
- Remove one strip from the bottle and replace the cap immediately.
- Immerse the reagent area of the strip in the urine specimen and take it out quickly.
- Wipe off excess urine against the rim of the specimen container.
- Read the test results carefully within 60 seconds in a good light and with the test area held near the appropriate color chart on the bottle label. Changes in color that appear only along the edges of the test pads or after moving than 2 minutes have passed are of no diagnostic significance. Results with leukocytes test portion can be read within 120 seconds.
If reading instrumentally, carefully follow the directions given in the appropriate instrument operating manual.
Ambient temperature: 20-30°C, relative humidity≤80%, the best test temperature: 23-27°C
Store between 2-30°C in dry condition. Keep away from refrigerator direct sunlight. Do not touch test area of reagent strips. Isolated from damp, light and high temperature for the aim of preserving the reaction activity of reagent.
Limitation of Procedures
Just like all the laboratory tests, the diagnosis results and treatment protocols cannot be decided only by any single diagnostic method.
Leukocytes: Prrole phenol lipid and the neutrophil esterase under the hydrolysis, produces free phenol, the free phenol coupled reacts with arenediazonium salts, produce purple azo dyes.
Nitrite: Nitrite and aromatic amino-sulfanilamide react to diazo compound, and the diazo compound coupled reacts with tetrahydro-benzoquinoline-3-phenol, which produces azo dyes.
Urobilinogen: Urobillinogen and diazonium salt coupled react to purplish red compounds.
Protein: The protein based on a certain indicator negative charge attracts protein cationic, ionizing causes the color change.
pH: Applied to acid alkali indicator method.
Blood: Hemoglobin acts as peroxides. It can cause peroxidase release new-born , which causes the color change.
Specific Gravity: methyl vinyl ether, maleic copolymer are weak acid (-COOH) ion exchange bodies, and the electrolyte ( M+ X- ) in the form of salt in urine, the M+ (main are Na+) reacts with ion exchange bodies, produces hydrogen ion, hydrogen ion reacts with acid-base indicator, then the color change.
Ascorbic Acid: Ascorbic Acid has 1,2-enediol reducing genes, the oxidation state blue 2,6-dichlorophenol indophenol is reduced 2,6- dichloro phenol amine.
Ketone: The acetoacetate and sodium nitroprusside cause reaction in alkaline medium, which produces purplish red compounds.
Bilirubin: The direct bilirubin and dichlorobenzene diazonium coupled react to azo dyes in acid medium.
Glucose: The glucose catalyzes the gluconate and peroxide hydrogen under the action of the glucose oxidase. Hydrogen peroxide catalyzes new-born , oxide potassium iodide, then the color change.
Microalbumin: with tolerance principle, use the high sensitive sulfonephthalein dye.
(based on dry weight at time of impregnation)
|Leukocytes||pyrrole amino acid esterdiazonium salt
|Nitrite||p-arsanilic acidtetrahydro benzoquinoline
|Urobilinogen||p-diethylamino benzaldehydenon-reaction ingredients||0.2%W/W99.8%W/W|
|pH||methyl redbromthymol blue
|Specific Gravity||bromothymol bluepoly (methyl vinyl ether co maleic anhydride)||2.8%W/W97.2%W/W|
|Ascorbic Acid||2,6 dichlorophenol indophenolsnon-reaction ingredients||0.5%W/W99.5%W/W|
|Bilirubin||2,4-dichloroaniline diazonium saltbuffer
|Glucose||glucose oxidase (microbial, 123U)peroxidase (horseradish, 203U)
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